Vitamin c may ward off Post-Surgery pain syndrome
NCT ID NCT02390505
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether taking vitamin C before and after planned upper limb surgery could prevent complex regional pain syndrome (CRPS), a chronic pain condition. Nearly 1,000 adults participated, receiving either vitamin C or a placebo. The goal was to see if vitamin C reduces CRPS occurrence at 6 months after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Vitamin C
- What this could lead to
- If it works, this could provide a simple, low-cost way to prevent a painful chronic condition after upper limb surgery.
- What could go wrong
- The trial is completed but results are not yet widely known. Vitamin C may not reduce CRPS risk, and individual factors like allergies or hemochromatosis could limit its use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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995 people
The number who actually took part.
- Started
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Jul 2016
- Finished
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Dec 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patients over 18 yo * patients undergoing major surgery of the upper limb * patients able to give their consent to follow the protocol of treatment and monitoring. Exclusion Criteria: * children, * patients under guardianship, * pregnant or lactating women, * patients with hemochromatosis, * allergy or known hypersensitivity to one of the molecules of treatment, * patients suffering or having already suffered from complex regional pain syndrome type 1 or type 2, * patients unable due to personal or professional mobility, to conduct post-operative follow up, * patients undergoing surgery with nerve suture with nerve graft, emergency surgery, * patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency, * patients with chronic kidney disease
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
CH Saint-Quentin
Saint-Quentin, 02321, France
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CHU Amiens
Amiens, 80054, France
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CHU Rouen
Rouen, 76031, France